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CABP2

calcium binding protein 2

HCNC Approved Symbol
CABP2 (HGNC:1385)
Genomic Coordinates
11:67,518,912 - 67,523,446 (11q13.2)
Synonyms
DFNB93
Disease Associations
This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

1Patient

In total, 1 patient was diagnosed with a variant in the CABP2 gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

Hearing loss
 1 (100.0%)
CABP2 - Gene browser | 3billion